Job Opportunities

Clinical Trial Associate

Reports to: VP, Head of Clinical Operations
Location: Plainsboro, NJ

About PMV Pharmaceuticals

PMV Pharma is a precision oncology company pioneering the discovery and development of small molecule, tumor-agnostic therapies targeting the reactivation of p53 mutants. p53 mutations are found in approximately half of all cancers. The field of p53 biology was established by our co-founder Dr. Arnold Levine when he discovered the p53 protein in 1979. Bringing together leaders in the field to utilize over four decades of p53 biology, PMV Pharma combines unique biological understanding with pharmaceutical development focus.  PMV Pharma is headquartered in Cranbury, New Jersey. For more information, please visit

Key Clinical Operations support role; ensures that delegated components of clinical trials are executed to expected and specified quality standards

Key Responsibilities

  • Provide high quality assistance supporting clinical trials according to applicable regulatory requirements and SOPs, within budget and timelines
  • Support the clinical team on project related activities and deliverables  
  • Assist in vendor oversight activities as applicable (e.g. collection or performance metrics, meeting minutes, etc.)
  • Contribute to the development of study specific documents, plans, and tools (e.g. ICFs, pharmacy manual, dosing diaries, study trackers, etc..) 
  • Assists in the distribution of study materials and Investigator/Site communications as applicable
  • Biological Sample management, oversight, and tracking:
    • Support in the development of laboratory specs and manuals 
    • Coordinate with labs on the tracking, analysis, and storage of samples
  • Supports contracts and budget activities (e.g. administrative activities related to invoice processing and change orders)
  • Study Trial Master File (TMF) maintenance support and oversight (including QC checks)
  • Prepare, ship, and manage inventory of study related supplies as needed
  • Other duties and assignments as requested for the overall performance of the function and Company


  • Highly motivated
  • Detailed oriented with a view to overall scope of the project
  • Organized
  • Accountable


  • BA/BS degree or higher
  • 1-2 years related experience, preferably in the pharmaceutical industry or equivalent
  • Possess a general understanding of clinical trials, the drug development process, and ICH GCP strongly preferred
  • Strong attention to detail and meticulous follow-through
  • Ability to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and procedures in a fast-paced environment
  • Proficiency using Microsoft Outlook, Word, PowerPoint, and Excel
  • Exceptional oral, written, and interpersonal skills

How to Apply

To apply, please submit your cover letter and resume to


PMV Pharmaceuticals is an Equal Opportunity Employer and all applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.